14143-32-9 Usage
Uses
Used in Pharmaceutical Research:
4-Chloro-3-ethylphenol is used as a research tool for the investigation of ryanodine receptors, which are crucial in the regulation of calcium release in cells. Understanding these receptors can lead to advancements in the treatment of various diseases and conditions.
Used in Diagnostics for Malignant Hyperthermia:
4-Chloro-3-ethylphenol is utilized as a diagnostic reagent for malignant hyperthermia, a potentially life-threatening condition that affects muscle cells and is often triggered by exposure to certain anesthetics and stress agents. Its role in diagnostics helps in the early detection and management of this condition.
Used in Chemical Synthesis:
As an organic compound, 4-Chloro-3-ethylphenol can also be used as an intermediate in the synthesis of various chemical products, including pharmaceuticals, agrochemicals, and other specialty chemicals, where its unique structure contributes to the desired properties of the final product.
Used in Analytical Chemistry:
4-Chloro-3-ethylphenol can be employed in analytical chemistry as a reference material or standard for the development and validation of analytical methods, particularly those involving the detection and quantification of related compounds or the assessment of ryanodine receptor activity.
Check Digit Verification of cas no
The CAS Registry Mumber 14143-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,4 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14143-32:
(7*1)+(6*4)+(5*1)+(4*4)+(3*3)+(2*3)+(1*2)=69
69 % 10 = 9
So 14143-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClO/c1-2-6-5-7(10)3-4-8(6)9/h3-5,10H,2H2,1H3
14143-32-9Relevant academic research and scientific papers
Process for preparing 2,4-dichloro-3-alkyl-6-nitrophenols
-
, (2008/06/13)
2-4-Dichloro-3-alkyl-6-nitrophenols which are useful as intermediate of cyan couplers in color photography are prepared by sulfonating 4-chloro-3-alkyl-phenols to obtain 5-chloro-4-alkylhydroxybenzenesulfonic acids, chlorinating the acids in an aqueous phase to obtain 3,5-dichloro-4-alkyl-2-hydroxybenzenesulfonic acids and nitrating the sulfonic acids.
